WO2021172564A1 - センサーおよびその製造方法 - Google Patents

センサーおよびその製造方法 Download PDF

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Publication number
WO2021172564A1
WO2021172564A1 PCT/JP2021/007534 JP2021007534W WO2021172564A1 WO 2021172564 A1 WO2021172564 A1 WO 2021172564A1 JP 2021007534 W JP2021007534 W JP 2021007534W WO 2021172564 A1 WO2021172564 A1 WO 2021172564A1
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WIPO (PCT)
Prior art keywords
protective film
probe
film
reagent layer
electrode
Prior art date
Application number
PCT/JP2021/007534
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English (en)
French (fr)
Japanese (ja)
Inventor
史徳 忽那
雅樹 藤原
将美 富岡
池田　俊弘
松井　昌朋
眞人 末吉
Original Assignee
Ｐｈｃホールディングス株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ｐｈｃホールディングス株式会社 filed Critical Ｐｈｃホールディングス株式会社
Priority to CN202180016592.4A priority Critical patent/CN115151190A/zh
Priority to EP21761274.6A priority patent/EP4111967A4/en
Priority to JP2022503369A priority patent/JP7316437B2/ja
Priority to US17/800,100 priority patent/US20230105478A1/en
Publication of WO2021172564A1 publication Critical patent/WO2021172564A1/ja

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/145—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue
    • A61B5/1468—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue using chemical or electrochemical methods, e.g. by polarographic means
    • A61B5/1486—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue using chemical or electrochemical methods, e.g. by polarographic means using enzyme electrodes, e.g. with immobilised oxidase
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/145—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue
    • A61B5/1468—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue using chemical or electrochemical methods, e.g. by polarographic means
    • A61B5/1486—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue using chemical or electrochemical methods, e.g. by polarographic means using enzyme electrodes, e.g. with immobilised oxidase
    • A61B5/14865—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue using chemical or electrochemical methods, e.g. by polarographic means using enzyme electrodes, e.g. with immobilised oxidase invasive, e.g. introduced into the body by a catheter or needle or using implanted sensors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/145—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue
    • A61B5/14532—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue for measuring glucose, e.g. by tissue impedance measurement
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
    • A61B5/6846—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be brought in contact with an internal body part, i.e. invasive
    • A61B5/6847—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be brought in contact with an internal body part, i.e. invasive mounted on an invasive device
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B2562/00—Details of sensors; Constructional details of sensor housings or probes; Accessories for sensors
    • A61B2562/12—Manufacturing methods specially adapted for producing sensors for in-vivo measurements
    • A61B2562/125—Manufacturing methods specially adapted for producing sensors for in-vivo measurements characterised by the manufacture of electrodes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/0002—Remote monitoring of patients using telemetry, e.g. transmission of vital signals via a communication network

Definitions

  • This disclosure relates to a sensor and its manufacturing method.
  • the CGM sensor includes a bioprotective film that covers a reagent layer containing an oxidoreductase or the like.
  • the thickness of the protective film is different for each sensor, the performance of the sensor will vary. Therefore, there is a demand for a sensor that can be easily manufactured and that suppresses variations in performance.
  • the non-limiting examples of the present disclosure contribute to the provision of a sensor capable of easily forming a protective film and suppressing variations in performance, and a method for manufacturing the same.
  • the sensor according to an embodiment of the present disclosure is a sensor that has a probe that is inserted into a living body and measures an analysis, and the probe includes a substrate, an electrode formed on the substrate, and the same. It has a reagent layer formed on an electrode, a first protective film formed on the reagent layer, and a second protective film formed on the first protective film, which is thinner than the first protective film. ..
  • the method for manufacturing a sensor is a method for manufacturing a sensor that has a probe to be inserted into a living body and measures an analysis, and the probe has an electrode on a sheet-like substrate.
  • the substrate is immersed in a protective film solution, and a second protective film thinner than the first protective film is formed on the first protective film.
  • the senor can be easily manufactured and the variation in performance can be suppressed.
  • FIG. 5 is a cross-sectional view taken along the line DD Perspective view of the reagent layer portion of the probe Top view of the tip of the probe.
  • FIG. 5 is a cross-sectional view taken along the line DD Perspective view of the reagent layer portion of the probe Top view of the tip of the probe.
  • the figure which showed the example of the opening shape of a film The figure explaining an example of the size of a sensor Perspective view of the sensor probe according to the second embodiment Partial side view of the probe of FIG. 13 as viewed from the third surface side Partial side view of the probe on which the protective film is formed as viewed from the third surface side Partial side view of the probe on which the protective film is formed as viewed from the third surface side
  • the figure explaining an example of the manufacturing method of a probe The figure explaining an example of the manufacturing method of a probe
  • the figure explaining an example of the manufacturing method of a probe The figure explaining an example of the manufacturing method of a probe
  • the figure explaining an example of the manufacturing method of a probe The figure explaining an example of the manufacturing method of a probe Partial side view of the probe on which the protective film is formed as viewed from the third surface side Top view of the tip of the probe of FIG.
  • Partial side view of the probe on which the protective film is formed as viewed from the third surface side The figure explaining an example of the manufacturing method of a probe The figure explaining an example of the manufacturing method of a probe The figure explaining an example of the manufacturing method of a probe The figure explaining an example of the manufacturing method of a probe The figure explaining the shape example of the 1st protective film 51 formed in step H
  • FIG. 1 is a diagram showing an application example of the sensor 1 according to the first embodiment.
  • FIG. 1 shows a living body 2 in addition to the sensor 1.
  • the living body 2 is, for example, a human body.
  • the sensor 1 shown in FIG. 1 is, for example, a biosensor. More specifically, the sensor 1 is a CGM sensor. In the sensor 1, the probe included in the sensor 1 is inserted into the living body 2, and the glucose concentration in the blood or interstitial fluid of the living body 2 is continuously or semi-continuously measured. For example, the sensor 1 measures the glucose concentration of the living body 2 for several days to several weeks.
  • FIG. 2 is a cross-sectional view of the sensor 1.
  • the same components as those in FIG. 1 are designated by the same reference numerals.
  • the senor 1 has a main body 11 and a probe 12.
  • the probe 12 is inserted into the living body 2.
  • the probe 12 has a reagent layer containing an oxidoreductase, and outputs an electric signal based on the glucose concentration to the main body 11.
  • the main body 11 stores an electric signal based on the glucose concentration output from the probe 12 in a storage device, and transmits the electric signal to another device (not shown) at a predetermined timing.
  • FIG. 3 is a plan view of the probe 12.
  • FIG. 3A shows the entire probe 12.
  • FIG. 3B shows an enlarged view of the tip portion of the probe 12 shown in FIG. 3A.
  • the portion of the probe 12 region X1 (head of the probe 12) shown in FIG. 3A is housed in the main body 11.
  • the tip portion of the probe 12 projects from the main body 11.
  • the tip portion of the probe 12 is inserted into the living body 2.
  • the arrow X2 shown in FIG. 3A indicates the direction in which the probe 12 is inserted into the living body 2.
  • the probe 12 has a substrate 21, an electrode 22, a reagent layer 23, a reference layer 24, and a film 25.
  • the manufacturing method of the probe 12 will be outlined.
  • the electrode 22 is formed on the substrate 21.
  • the substrate 21 is, for example, a sheet-shaped synthetic resin.
  • the electrodes 22 are uniformly formed on the substrate 21.
  • the material of the electrode 22 is, for example, gold (Au).
  • the electrode 22 may be formed on the substrate 21 by, for example, sputtering.
  • the electrode 22 may be referred to as an electrode film or an electrode layer.
  • the electrode 22 is separated into three regions. Grooves A1 and A2 are formed in the electrodes 22 formed on the substrate 21, and the electrodes 22 are separated into three regions.
  • the electrode 22 is separated into an working electrode 22a, a reference electrode 22b, and a counter electrode 22c by grooves A1 and A2.
  • the grooves A1 and A2 may be formed by, for example, laser trimming.
  • the working pole 22a may be referred to as a working pole membrane or working pole layer.
  • the reference electrode 22b may be referred to as a reference electrode membrane or a reference electrode layer.
  • the counter electrode 22c may be referred to as a counter electrode membrane or a counter electrode layer.
  • the working electrode 22a has a potential (reference electrode) sufficient to oxidize, for example, a mediator (including hydrogen peroxide as well as an electronic mediator) reduced by a reaction of an analysis (glucose) with an oxidoreductase.
  • a potential reference electrode
  • Glucose concentration is measured by monitoring the current flowing between the working electrode 22a and the counter electrode 22c.
  • the reference layer 24 is formed.
  • a reference layer 24 is formed on the reference electrode 22b at the tip of the probe 12.
  • the material of the reference layer 24 is, for example, silver / silver chloride (Ag / AgCl).
  • the reference layer 24 may be formed by a screen printing method or an inkjet method using, for example, Ag / AgCl paste (ink).
  • the reference layer 24 may be referred to as a reference membrane or a reference electrode.
  • the film 25 is arranged and fixed.
  • a film 25 having an opening is arranged on the working electrode 22a, the reference electrode 22b, the counter electrode 22c, and the reference layer 24 formed on the substrate 21.
  • the film 25 is in the form of a sheet and has an insulating property.
  • the film 25 is arranged so that the opening portion is located at the tip portion (the portion forming the reagent layer 23) of the probe 12. A reagent described later is dropped into the opening of the film 25.
  • the film 25 may be referred to as a film layer, an insulating layer, or an insulating film. Arrangement may be paraphrased as stacking or placement.
  • the film 25 has an opening so that the upper surface of the counter electrode 22c (the surface in the front side direction of the paper surface in FIG. 3) is partially exposed.
  • the opening of the film 25 has a notch shape as shown in the region X3 of FIG. 3 (B) by the cutting step of (7) described later. Due to this notch shape, the counter electrode 22c is partially exposed on the upper surface.
  • the upper surface may be regarded as the surface on the side where the reagent layer 23 of the probe 12 is formed.
  • the film 25 has a shape in which the head portion of the probe 12 is partially exposed.
  • the portion of region X4 in FIG. 3A is not covered by the film 25.
  • the exposed electrode 22 in the region X4 is connected to the circuit of the main body 11.
  • the upper surface of the reference layer 24 is covered with the film 25 as shown in FIG. 3B.
  • the reference layer 24 is exposed in the width direction of the probe 12 (perpendicular to the insertion direction indicated by the arrow X2).
  • the reference layer 24 is exposed on the right side surface of the tip portion of the probe 12 (see also the reference layer 24 of FIG. 4B).
  • the reagent layer 23 is formed.
  • a reagent layer 23 is formed on the working electrode 22a at the tip of the probe 12.
  • the reagent is dropped into the opening of the film 25 described above and dried to form the reagent layer 23.
  • the reagent layer 23 is not formed at the tip of the probe 12 shown by the arrow X5 in FIG. 3 (B).
  • the reagent layer 23 is preferably formed away from the tip of the probe 12. That is, it is preferable that the reagent layer 23 is not formed over a predetermined distance from the tip of the probe 12. This is because by forming the reagent layer 23 away from the tip of the probe 12, it is possible to prevent the reagent layer 23 from peeling off (turning over) from the probe 12 when the probe 12 is inserted into the living body 2.
  • the reagent layer 23 contains at least an oxidoreductase capable of a redox reaction with analite (glucose).
  • the reagent layer 23 may be referred to as a reagent membrane, a working layer, or a working electrode.
  • the opening of the film 25 may have, for example, a size and a shape in which a reagent layer 23 having a width larger than the width of the probe 12 is formed.
  • the shape of the reagent layer 23 formed to be larger than the width of the probe 12 is shaped by the next trimming step.
  • the reagent layer 23 and the electrode 22 are removed.
  • the reagent layer 23 and the electrode 22 are trimmed along the insertion direction of the probe 12 at the end portion in the width direction of the probe 12 whose outer shape is formed by the cutting step (7) described later.
  • the upper surface of the substrate 21 is partially exposed as shown in the region X6 of FIG. 3 (B).
  • laser trimming may be used for trimming the reagent layer 23 and the electrode 22.
  • the film 25 is also partially (slightly) trimmed at both ends in the insertion direction of the reagent layer 23.
  • the probe 12 is cut out from the substrate 21 by cutting.
  • the substrate 21 that has undergone the steps (1) to (6) above is cut, and the probe 12 having the shape shown in FIG. 3 (A) is cut out.
  • the cutting position includes the trimmed part. For example, the vicinity of the center (near the center line) of the trimmed portion (bottom portion of the recess) is cut.
  • the tip portion of the cut probe 12 is attached to, for example, a liquid forming a protective film to form a protective film.
  • the protective film prevents or suppresses leakage of substances (mainly oxidoreductases and electron mediators) contained in the reagent layer 23 to the outside of the protective film.
  • the protective film has pores through which the analite existing outside the protective film permeates into the protective film in which the reagent layer 23 is present.
  • the protective film only needs to be able to protect (coat) at least the portion of the reagent layer 23 of the probe 12.
  • FIG. 4A is a cross-sectional view taken along the line AA of FIG. As shown in FIG. 4A, in the portion of the probe 12 where the reagent layer 23 is formed, the working electrode 22a is formed on the substrate 21 (upper surface). The reagent layer 23 is formed on the working electrode 22a.
  • the reagent layer 23 and the working electrode 22a are removed at both ends in the width direction (side surface of the probe 12) of the probe 12 by the trimming step of (6) above.
  • the cutting step of (7) above the substrate 21 exposed by the trimming step of (6) above is cut at a position away from the reagent layer 23 and the working electrode 22a.
  • the side surface of the probe 12 becomes stepped as shown by arrows 11a and 11b in FIG. 4A.
  • a protective film is formed around the tip of the reagent layer 23 of the probe 12. In FIG. 4A, the protective film is not shown.
  • FIG. 4B is a cross-sectional view taken along the line BB of FIG. As shown in FIG. 4B, in the portion where the reference layer 24 of the probe 12 is formed, the working electrode 22a and the reference electrode 22b are formed on the substrate 21. The working pole 22a and the reference pole 22b are physically and electrically separated by the groove A1.
  • the reference layer 24 is formed on the reference pole 22b.
  • the film 25 is arranged on the working electrode 22a, the reference electrode 22b, and the reference layer 24.
  • the upper surface of the reference layer 24 is covered with the film 25, but is exposed on the side surface of the probe 12 (the right side surface in FIG. 4B).
  • the film 25 above the reference layer 24 may be omitted. That is, the upper surface of the reference layer 24 may be exposed.
  • FIG. 4C is a cross-sectional view taken along the line CC of FIG. As shown in FIG. 4C, in the portion where the upper surface of the counter electrode 22c is exposed, the working electrode 22a, the reference electrode 22b, and the counter electrode 22c are formed on the substrate 21.
  • the working pole 22a and the reference pole 22b are physically and electrically separated by the groove A1.
  • the reference electrode 22b and the counter electrode 22c are physically and electrically separated by the groove A2.
  • a film 25 is formed on the working electrode 22a and the reference electrode 22b.
  • the film 25 is not arranged on the counter electrode 22c, and the upper surface of the counter electrode 22c is exposed.
  • the substrate 21 is a synthetic resin on a sheet.
  • PET polyethylene terephthalate
  • it is not particularly limited as long as it is a resin material such as a plastic material having at least one of the characteristics of flexibility, easy workability, and heat resistance.
  • Other examples include general purpose plastics such as polyethylene, polypropylene, and polyethylene naphthalate.
  • polyimide is preferable.
  • Electrode 22 As described above, gold may be used as the material of the electrode 22. However, it is not particularly limited as long as it is a metal having conductivity and stability (for example, hard to oxidize or salt resistance) or a carbon material.
  • examples of the material of the electrode 22 include platinum, palladium, and carbon.
  • the metal material may be vapor-deposited (including sputtering) on the substrate 21.
  • Other forming methods include printing, plating, spin coating and the like.
  • carbon paste may be printed to form the electrode 22.
  • different electrode materials may be used for the working electrode and the counter electrode.
  • the reagent layer 23 contains at least an oxidoreductase capable of a redox reaction with analite. If the redox enzyme is a dehydrogenase, an electron mediator is further included. Further, the redox enzyme may be an oxidase (oxidase) or a system using an electron mediator. That is, if it is a system that electrochemically detects hydrogen peroxide generated by the redox reaction of glucose by an oxidase, an electron mediator is unnecessary, but it can also be detected electrochemically by using an electron mediator. In this case, the reagent layer 23 contains an electron mediator in addition to the oxidase.
  • examples of redox enzymes include glucose oxidase and glucose dehydrogenase.
  • glucose dehydrogenase flavin adenine dinucleotide (FAD) -linked glucose dehydrogenase is desirable from the viewpoint of low reactivity to maltose, and for example, enzymes derived from Aspergillus (Orize and Teres) and Mucor are preferable.
  • FAD flavin adenine dinucleotide
  • Examples of the electronic mediator include osmium complex, ruthenium complex, quinone compound, phenazine compound, ferrocene compound and the like. In addition, examples of the electronic mediator include derivatives of these.
  • silver / silver chloride As the material of the reference layer 24, silver / silver chloride (Ag / AgCl) may be used as described above.
  • the reference layer 24 may be formed by screen-printing or applying Ag / AgCl paste (ink) on the electrode 22 and then drying it.
  • Ag / AgCl paste As another forming method, silver (Ag) may be printed, coated, plated or the like on the electrode 22, and then the surface may be chlorinated to form the electrode 22.
  • the senor 1 shows an example of a three-electrode configuration of an working electrode, a counter electrode, and a reference electrode that realizes more accurate measurement, even if it is a two-electrode configuration of the working electrode and the counter electrode. good.
  • ⁇ Film 25 As the film 25, a sheet made of the same material as the substrate 21 to which an adhesive sheet (for example, acrylic type, rubber type, or hot melt type) is attached may be used. Further, a sheet made of a material different from that of the substrate 21 may be used. Further, the adhesive sheet alone may be used as the film 25. A thermal / thermoplastic resist film may be used as the film 25.
  • an adhesive sheet for example, acrylic type, rubber type, or hot melt type
  • the contact angle with the liquid on the film is preferably higher than the contact angle with the liquid at the opening, and the larger the difference, the more preferable.
  • the temperature on the film is 90 ° or more and the opening is 50 ° or less. Even if the material does not have such a contact angle, it is possible to have the contact angle by applying at least one of a water-repellent treatment to the film surface and a hydrophilic treatment to the opening.
  • the film 25 has a thickness of 1 ⁇ m or more and 150 ⁇ m or less, preferably 3 ⁇ m or more and 50 ⁇ m or less, and more preferably 5 ⁇ m or more and 30 ⁇ m or less.
  • the film 25 may be formed by printing a resist ink.
  • the protective film covering the surface of the reagent layer 23 has biocompatibility in which proteins and cells are not adsorbed or proteins and cells are not easily adsorbed.
  • the protective film is preferably formed of a polymer having the above-mentioned properties.
  • polymer examples include a copolymer of methyl methacrylate and hydroxyethyl methacrylate, a copolymer of butyl methacrylate and hydroxyethyl methacrylate, poly (2-methacryloyloxyethyl phosphorylcholine-con-butyl methacrylate) and the like.
  • high molecular weight polymer examples include (meth) acrylate compounds having the same main chain as these exemplified polymers and having a reactive group capable of reacting with the linker in the side chain. It can also be used as an "ethylene-based polymer" having a methacryloyl group or an acryloyl group.
  • FIG. 5 is a diagram for explaining the positional relationship between the reagent layer 23 and the film 25.
  • FIG. 5 shows a plan view of the tip portion of the probe 12.
  • the same components as those in FIG. 3 are designated by the same reference numerals.
  • FIG. 5 shows a part of the manufacturing process of the probe 12.
  • the “film formation” shown in FIG. 5 corresponds to the step (4) described above.
  • “Applying the reagent solution” and “drying the applied reagent solution” correspond to the step (5) described above.
  • “Trimming” corresponds to the step (6) described above.
  • “Sensor cutting” corresponds to the step (7) described above.
  • the “protective film formation” corresponds to the step (8) described above.
  • FIG. 6 is a cross-sectional view taken along the line DD of FIG.
  • a film 25 having an opening is arranged on the working electrode 22a. Then, the reagent is dropped onto the opening portion of the film 25 and dried. As a result, the reagent layer 23 is sandwiched and formed between the films 25 in the insertion direction of the probe 12, as shown in FIG. That is, the reagent layer 23 fits and is formed in the region defined by the opening of the film 25. In other words, the film 25 is adjacent to the reagent layer 23 on the electrode 22.
  • the film 25 on the insertion direction side does not have to be formed.
  • the film 25 on the left side shown in FIGS. 5 and 6 may be omitted.
  • FIG. 7 is a perspective view of the reagent layer 23 portion of the probe 12.
  • the probe 12 faces the upper surface 31 on which the reagent layer 23 is formed, the back surface 32 facing the upper surface 31, the side surface 33 connecting the upper surface 31 and the back surface 32, and the side surface 33. It has a side surface 34 that connects the upper surface 31 and the back surface 32.
  • the arrow X2 shown in FIG. 7 indicates the insertion direction of the probe 12 into the living body 2.
  • the end of the upper surface 31 in the width direction of the probe 12 has stepped trimming portions 35 and 36 from which the reagent layer 23 and the electrode 22 have been removed.
  • the trimming portions 35 and 36 are formed at least in a positional relationship in contact with the reagent layer 23.
  • the reagent layer 23 extends from end to end in the width direction of the upper surface 31 to form the upper surface 31 of the probe 12 and forms a part of the side surface of the probe 12 (reagent layer of FIG. 4A). See also 23).
  • the above sensor 1 may be regarded as having the following components.
  • the sensor 1 has a main body 11 and a probe 12.
  • the probe 12 is inserted into the living body 2 and acquires an electric signal for continuously or semi-continuously measuring the analyst.
  • the substrate 21 has a first surface (for example, an upper surface 31) and a second surface (for example, a back surface 32) facing the first surface. Further, the substrate 21 has a third surface and a fourth surface (for example, side surfaces 33 and 34) of a surface that connects the first surface and the second surface and extends in the insertion direction of the probe 12.
  • the working electrode 22a is formed on the first surface of the substrate 21 in the first electrode material.
  • the reagent layer 23 is arranged in a part of the working electrode 22a.
  • the trimming portions 35 and 36 are formed by removing the reagent layer 23 and the first electrode material at both ends of the first surface in a direction orthogonal to the direction in which the probe 12 is inserted into the living body 2. ..
  • the reagent layer 23 contains an oxidoreductase.
  • the trimming portions 35 and 36 are formed in a positional relationship of at least in contact with the reagent layer 23.
  • the film 25 is adjacent to the reagent layer 23 in the direction of insertion into the living body 2 in the direction opposite to the tip end side of the probe 12.
  • the reagent layer 23 does not have a portion sandwiched between the electrode 22 and the film 25.
  • the film 25 is not placed on the reagent layer 23.
  • the film 25 may or may not be adjacent to the reagent layer 23 on the distal end side of the probe 12. In other words, the film 25 may or may not be formed on the distal end side of the probe 12.
  • the above sensor 1 may be regarded as having the following manufacturing process.
  • a substrate 21 (substrate sheet) in which the working electrode 22a of the first electrode material is formed on the first surface is prepared.
  • the reagent solution is dried to form the reagent layer 23.
  • a predetermined position of the reagent layer 23 on the substrate 21 is trimmed to form a trimming portion from which the working electrode 22a formed under the reagent layer 23 and the reagent layer 23 has been removed.
  • the substrate 21 is cut into a predetermined shape (the shape of the probe 12 shown in FIG. 3A, for example, the shape of a flagpole).
  • the trimming portions 35 and 36 are included in the positions where the substrate 21 is cut.
  • a protective film may be formed at the tip of the probe 12 on which the reagent layer 23 is formed.
  • the protective film has pores that allow at least an analysis (glucose) to pass through.
  • the counter electrode 22c may be formed on the first surface of the substrate 21 or may be formed on the second surface.
  • Another counter electrode (second counter electrode) different from the counter electrode 22c may be formed on both or one of the first surface and the second surface of the substrate 21.
  • the reference electrode 22b may be formed on at least one of the first to fourth surfaces.
  • the film 25 may be arranged on the upper surface and the third surface side may be exposed.
  • the reagent layer 23 does not have to be formed over a predetermined distance from the terminal side (tip of the probe 12) of the first surface in the insertion direction of the probe 12.
  • a part (end) of the reagent layer 23 may be sandwiched between the electrode 22 and the film 25.
  • the reagent layer 23 does not have to have a portion sandwiched between the electrode 22 and the film 25.
  • the sensor 1 has a probe 12 inserted into the living body 2 and measures the analyst.
  • the probe 12 has a substrate 21, an electrode 22 formed on the substrate 21, and a reagent layer 23 containing an oxidoreductase and formed on the electrode 22.
  • the reagent layer 23 and the electrode 22 are trimmed along the insertion direction of the probe 12 into the living body 2.
  • the variation in performance of the sensor 1 caused by the manufacturing process is suppressed.
  • a uniform (uniform) portion in the ring is used as the reagent layer 23 by trimming. Available.
  • the cutting edge when cutting into the probe 12 shape, the cutting edge can be prevented from coming into contact with the reagent layer 23, and cracking of the reagent layer 23 can be reduced.
  • the cutting edge when cutting into the probe 12 shape, the cutting edge can be prevented from coming into contact with the reagent layer 23, and contamination of the reagent can be suppressed.
  • the probe 12 included in the sensor 1 has a step of forming the electrode 22 on the substrate 21, a step of forming the reagent layer 23 containing the oxidoreductase on the electrode 22, and the width of the probe 12.
  • Manufactured by a step of trimming the reagent layer 23 and the electrode 22 along the insertion direction of the probe 12 into the living body 2 at at least one end in the direction.
  • the variation in performance of the sensor 1 caused by the manufacturing process is suppressed.
  • a uniform (uniform) central portion in the ring can be used as the reagent layer 23 by trimming.
  • the cutting edge when cutting into the shape of the probe 12, the cutting edge can be prevented from coming into contact with the reagent layer 23 by trimming, so that cracking of the reagent layer 23 can be reduced. In addition, contamination of reagents can be suppressed.
  • the film 25 is arranged on the electrode 22 so as to be adjacent to the reagent layer 23 at both ends in the insertion direction of the reagent layer 23.
  • the film 25 can determine the position where the reagent is dropped, and a uniform reagent layer 23 can be formed before trimming.
  • the probe 12 may have a trimming section at one end in the width direction. That is, the number of trimming portions may be one.
  • FIG. 8 is a plan view of the tip portion of the probe 12.
  • the same components as those in FIG. 3 are designated by the same reference numerals.
  • FIG. 8 shows an example in which the working electrode 22a and the counter electrode 22c are formed side by side in the width direction of the probe 12. In FIG. 8, the film 25 is not shown.
  • the reagent layer 23 is formed so as to straddle the width of the probe 12 on one end side in the width direction of the probe 12.
  • the reagent layer 23 is formed on the other end side in the width direction of the probe 12 so as not to straddle the width of the probe 12.
  • the reagent layer 23 is formed so as to straddle the right end of the probe 12 and not to straddle the left end of the probe 12.
  • the probe 12 has a trimming portion 41.
  • the trimming portion 41 is formed on the side where the reagent layer 23 straddles the width of the probe (on the right side in FIG. 6).
  • the trimming portion 41 is formed by trimming the reagent layer 23 and the working electrode 22a.
  • the trimming section 41 exposes the substrate 21.
  • the probe 12 may have a trimming portion at one end in the width direction. This also suppresses the variation in performance of the sensor 1 caused by the manufacturing process.
  • the reagent layer 23 may protrude outside the region defined by the film 25 in the insertion direction of the probe 12.
  • FIG. 9 is a diagram for explaining the positional relationship between the reagent layer 23 and the film 25.
  • FIG. 9 shows a plan view of the tip portion of the probe 12.
  • the same components as those in FIG. 3 are designated by the same reference numerals.
  • FIG. 9 shows a part of the manufacturing process of the probe 12.
  • “Applying the reagent solution” and “drying the applied reagent solution” shown in FIG. 9 correspond to the step (5) described above.
  • the “film formation” corresponds to the step (4) described above.
  • “Trimming” corresponds to the step (6) described above.
  • “Sensor cutting” corresponds to the step (7) described above.
  • the “protective film formation” corresponds to the step (8) described above.
  • FIG. 10 is a cross-sectional view taken along the line EE of FIG.
  • a film 25 having an opening is arranged on the reagent layer 23.
  • the film 25 is arranged so that the opening portion is located in the reagent layer 23.
  • the openings of the film 25 are formed so as to overlap the reagent layer 23 at both ends of the reagent layer 23 in the insertion direction (direction of arrow X2). That is, a part of the film 25 overlaps the reagent layer 23 at both ends of the reagent layer 23 in the insertion direction. Further, a part of the film 25 overlaps the trimming portion at both ends in the insertion direction of the trimming portion.
  • the film 25 on the insertion direction side does not have to be formed.
  • the film 25 on the left side shown in FIGS. 9 and 10 may be omitted.
  • the film 25 is arranged on the electrode 22 so as to overlap the reagent layer 23 and the trimming portion at both ends of the reagent layer 23 in the insertion direction.
  • the variation in performance of the sensor 1 caused by the manufacturing process is suppressed.
  • the end portion (edge portion of the coffee ring) of the reagent layer 23 in the insertion direction of the probe 12 can be covered with the film 25 to expose a uniform portion of the reagent layer 23.
  • FIG. 11 is a diagram showing an example of the opening shape of the film 25.
  • the hatched portions of FIGS. 11A and 11B indicate trimming portions.
  • the figures such as the polygonal shape and the round shape shown in (A) of FIG. 11 and (B) of FIG. 11 indicate the shape of the opening portion of the film 25.
  • the arrow X2 shown in FIG. 11 indicates the direction in which the probe 12 is inserted into the living body 2.
  • films 25 are formed at both ends of the reagent layer 23 in the insertion direction (see, for example, FIGS. 5 and 6).
  • a film 25 is formed at the end of the reagent layer 23 opposite to the tip end side (for example, the film 25 on the right side of FIGS. 5 and 6 is formed, and the film 25 on the left side is formed. Not done).
  • the opening shape of the film 25 may have various shapes.
  • FIG. 12 is a diagram illustrating an example of the size of the sensor 1.
  • the same components as those in FIGS. 3 and 7 are designated by the same reference numerals.
  • the film 25 is not shown.
  • the width D1 of the tip portion of the probe 12 is, for example, 70 ⁇ m or more and 1700 ⁇ m or less.
  • the width D1 is 70 ⁇ m or more and 600 ⁇ m or less, more preferably 70 ⁇ m or more and 400 ⁇ m or less.
  • the width D2 of the trimming portions 35 and 36 is, for example, 5 ⁇ m or more.
  • the width D2 is not particularly limited as long as it has a width that can secure the reagent layer 23 with respect to the width of the tip portion of the probe 12.
  • it can be realized by irradiating the laser a plurality of times.
  • the protective film covering the outer periphery of the probe will be described.
  • the protective film may be referred to as a bioprotective film.
  • the protective film has pores sized to allow small molecule compounds to pass through.
  • the protective membrane has pores sized to allow glucose as an analyst to permeate. As a result, glucose in the outside of the probe can permeate the protective membrane and reach the probe.
  • a sensor such as a CGM sensor embedded in a living body prevents a reagent in a reagent layer formed on the probe from leaking into the living body while measuring a glucose concentration or the like by a protective film.
  • the protective film may be formed (coated) at least on a portion covering the reagent layer. Therefore, the protective film may be formed by a dip method.
  • the protective film component is dissolved in an organic solvent such as ethanol, and the probe is immersed in the protective film solution.
  • an organic solvent such as ethanol
  • the formation of the protective film by the dip method is complicated in the manufacturing process.
  • the thickness and shape of the protective film vary from sensor to sensor, resulting in variations in performance.
  • the variation of the protective film can be suppressed, but the number of times of immersion and drying increases, which complicates the manufacturing process.
  • a protective film solution having a high concentration of protective film components is used to simplify the manufacturing process and the number of times of immersion and drying is reduced, the thickness and shape of the protective film vary, and the performance varies.
  • FIG. 13 is a perspective view of the probe 12 of the sensor 1 according to the second embodiment.
  • the same components as those in FIGS. 2 and 3 are designated by the same reference numerals.
  • the probe 12 shown in FIG. 13 has an electrode 22 like the probe 12 described in the first embodiment. Further, the probe 12 includes a reagent layer 23 (not shown in FIG. 13) and a reference layer 24 (not shown in FIG. 13), similarly to the probe 12 described in the first embodiment. The first surface has a counter electrode 22c (not shown in FIG. 13), which is partially exposed.
  • the surface of the probe 12 on which the reagent layer 23 and the reference layer 24 are formed may be referred to as a first surface.
  • the surface facing the first surface may be referred to as a second surface.
  • the direction from the second surface to the first surface (direction of arrow X2a in FIG. 13) may be referred to as a height direction.
  • a surface that connects the first surface and the second surface and extends in the insertion direction of the probe 12 (direction of arrow X2 in FIG. 13), and the surface on the right side when viewed from the tip of the probe 12 is the third surface. May be called.
  • a surface that connects the first surface and the second surface and extends in the insertion direction of the probe 12, and the surface on the left side when viewed from the tip of the probe 12 may be referred to as a fourth surface.
  • the surface of the probe 12 facing the insertion direction may be referred to as a tip surface.
  • the first surface may be referred to as the upper surface.
  • the second surface may be referred to as the bottom surface.
  • the third and fourth surfaces may be referred to as side surfaces.
  • FIG. 14 is a partial side view of the probe 12 of FIG. 13 as viewed from the third surface side.
  • FIG. 14 shows the probe 12 before the protective film described later is formed.
  • an electrode 22 is formed on the first surface side of the substrate 21.
  • the electrode 22 has an working electrode 22a, a reference electrode 22b, and a counter electrode 22c.
  • a reagent layer 23 is formed on the first surface side of the working electrode 22a of the electrode 22.
  • a reference layer 24 is formed on the first surface side of the reference electrode 22b of the electrode 22.
  • the reference layer 24 is formed by curing the Ag / AgCl paste applied on the reference electrode 22b.
  • the working electrode 22a at the tip of the probe 12 (the working pole 22a on the tip side of the probe 12 with the reagent layer 23 as a boundary) is covered with the film 25.
  • the film 25 covering the working electrode 22a at the tip of the probe 12 was in contact with the reagent layer 23, but may be separated as shown by the arrow A21 in FIG.
  • the film 25 has an opening in the portion corresponding to the reagent layer 23. As a result, the first surface side of the reagent layer 23 is exposed.
  • the first surface side of the reference layer 24 is covered with the film 25. In other words, the first surface side of the reference layer 24 is not exposed.
  • the reference layer 24 is exposed on the third surface side of the probe 12. In other words, the reference layer 24 is exposed in the width direction of the probe 12 (perpendicular to the insertion direction indicated by the arrow X2) (see also FIG. 4B).
  • the film 25 has an opening so that the portion in the region X3 on the first surface side of the counter electrode 22c is exposed.
  • the opening of the film 25 has a notch shape (see also region X3 in FIG. 3B). Due to this notch shape, the counter electrode 22c is partially exposed on the upper surface.
  • the portion of the working pole 22a from the head of the probe 12 (the portion of the region X1 in FIG. 13) to the reagent layer 23 may be referred to as a lead or a working pole lead.
  • the portion of the reference electrode 22b from the head of the probe 12 to the reference layer 24 may be referred to as a lead or a reference electrode lead.
  • the portion of the counter electrode 22c from the head of the probe 12 to the opening (region X3) of the film 25 may be referred to as a lead or counter electrode lead.
  • the reference layer 24 may be exposed on the fourth surface side. Further, the reference layer 24 and the counter electrode 22c may be formed on the second surface side. When the reference layer 24 and the counter electrode 22c are formed on the second surface side, the reference electrode lead and the counter electrode lead are formed on the second surface side.
  • FIG. 15 is a partial side view of the probe 12 on which the protective film is formed as viewed from the third surface side.
  • a first protective film 51 and a second protective film 52 are formed on the probe 12 of FIG.
  • the first protective film 51 and the second protective film 52 may be simply referred to as a protective film.
  • the first protective film 51 is formed so as to cover the reagent layer 23 formed on the working electrode 22a.
  • the first protective film 51 is formed so as to cover the first surface side, the third surface side, the fourth surface side, the tip surface side, and the surface side opposite to the tip surface side of the reagent layer 23. ..
  • the second protective film 52 covers the electrode 22, the reagent layer 23, the reference layer 24, and the film 25 formed on the substrate 21 (for example, so as to cover the tip portion of the probe 12 shown in FIG. 14). )It is formed.
  • the second protective film 52 includes a film 25 arranged at least on the working electrode 22a from the tip of the probe 12, a reagent layer 23 and a first protective film 51 formed on the working electrode 22a, and a reference electrode 22b. It is formed so as to cover the reference layer 24 and the film 25 arranged above and the film 25 having an opening arranged on the counter electrode 22c.
  • the second protective film 52 is formed so as to cover a portion from the tip of the probe 12 to a first predetermined distance exceeding at least the region X3.
  • the second protective film 52 may be formed on the first surface side, the second surface side, the third surface side, the fourth surface side, and the tip surface side of the probe 12.
  • the reagent layer 23 is formed at a position separated from the end of the probe 12 in the insertion direction into the living body by a predetermined distance. For example, as shown in FIG. 15, the reagent layer 23 is formed from a position separated from the tip of the probe 12 by a second distance.
  • the counter electrode 22c exposed from the opening (region X3) of the reference layer 24 and the film 25 is formed in a region opposite to the tip end side of the probe 12 with the reagent layer 23 as a boundary.
  • the first protective film 51 is formed by a sensor manufacturing method described later.
  • the first protective film 51 is formed by arranging a film formed of the protective film material so as to cover the reagent layer 23.
  • the first protective film 51 is not arranged from the tip of the probe 12 to the second predetermined distance. This is to make the tip of the probe 12 as thin as possible in consideration of the ease of insertion of the probe 12 into the living body. Further, if the first protective film 51 (including the reagent layer 23) is arranged at the tip of the probe 12, there is a possibility that the first protective film 51 (including the reagent layer 23) may dissociate when inserted into a living body.
  • the first protective film 51 is thicker than the second protective film.
  • the thickness of the first protective film 51 (the thickness of the first protective film 51 does not include the thickness of the second protective film 52 arranged on the first protective film 51) is determined in the height direction of the probe 12. It is thicker than the thickness of the second protective film arranged on the second predetermined distance on the first surface.
  • the first protective film 51 and the second protective film 52 allow the analytes existing outside the protective film to permeate into the protective film, while the outer protective film of the substance (mainly oxidoreductase) contained in the reagent layer 23. Since it is necessary to prevent or suppress leakage to, these protective membranes need only have pores of a size that allows sufficient permeation of analite and impermeability or difficulty of permeation of oxidoreductase, and are the same material. It may be a different material.
  • the first protective film 51 may be coated with the working electrode 22a including the reagent layer 23 as shown in FIG. 15, or may also be coated with the reference layer 24 as shown in FIG.
  • FIG. 16 is a partial side view of the probe 12 on which the protective film is formed as viewed from the third surface side.
  • the same components as in FIG. 15 are designated by the same reference numerals.
  • the first protective film 51 may also cover the reference layer 24.
  • the film 25 may not be arranged on the upper surface of the reference layer 24.
  • the first protective film 51 may also cover the counter electrode 22c (counter electrode 22c of the region X3 portion) exposed from the film 25.
  • the reference electrode 22b or the counter electrode 22c is arranged on the same surface as the working electrode 22a.
  • 17A-17D are diagrams illustrating an example of a method for manufacturing the probe 12.
  • step A a protective film sheet that serves as a base for the first protective film 51 is formed.
  • the protective film sheet may be referred to as a protective film film.
  • tBuMA4VP which is a protective film material
  • PEGDGE poly (ethylene glucol) diglycidyl ether
  • the protective film solution 61 is uniformly spread on the base material sheet 62 using the squeegee 63, and then dried. That is, a protective film as a base of the first protective film 51 is formed on the base sheet 62.
  • the thickness of the protective film formed on the base sheet may be, for example, 20 ⁇ m. If the predetermined thickness is not reached by spreading the coating once, the coating may be repeated a plurality of times.
  • the base material sheet After forming a protective film having a predetermined thickness, the base material sheet is cut into a shape having substantially the same diameter as the opening diameter (for example, ⁇ 3.5 mm) of step H described later.
  • the thickness of the protective film formed on the base sheet may be in the range of 5 ⁇ m or more and 60 ⁇ m or less. It is more preferably in the range of 10 ⁇ m or more and 45 ⁇ m or less, and further preferably in the range of 20 ⁇ m or more and 40 ⁇ m or less.
  • the protective film component concentration and the cross-linking agent concentration in the protective film solution are 1/4 or more and 1/2 or less by weight percent (w / v%) of the dissolution limit concentration of the protective film component with respect to the dissolving solvent.
  • the dissolution limit concentration of tBuMA4VP in ethanol is about 20%, it is preferably 5 w / v% or more and 10 w / v% or less.
  • the PEDGE concentration of the cross-linking agent is preferably 0.39 w / v% or more and 0.78% w / v or less because the dissolution limit in ethanol is about 1.55%.
  • the organic solvent to be dissolved ethanol is used in step A and step J described later, but it can dissolve the protective film solution and gives the influence of the oxidoreductase used (causes a large decrease in enzyme activity, etc.).
  • the soluble organic solvent is preferably an alcohol solvent.
  • the alcohol-based solvents a lower alcohol-based solvent (carbon chain is 6 or less) is preferable, and examples other than ethanol include methanol and isopropyl alcohol. Further, these organic solvents may be used in combination of a plurality of types.
  • Step B As shown in FIG. 17A (step B), the electrode 22 is formed on the substrate 21 on the sheet.
  • an electrode material such as gold is sputtered onto a sheet-shaped substrate 21 such as polyethylene terephthalate (PET) to form an electrode 22.
  • PET polyethylene terephthalate
  • Step C As shown in (Step C) of FIG. 17A, the working electrode 22a, the reference electrode 22b, and the counter electrode 22c are formed.
  • laser processing is used to form the working pole 22a, the reference pole 22b, and the counterpole 22c.
  • FIG. 17A shows an example in which the working electrode 22a, the reference electrode 22b, and the counter electrode 22c are formed on one surface.
  • the reference layer 24 is formed on the reference electrode 22b.
  • the reference layer 24 is formed by applying Ag / AgCl paste on the reference electrode 22b and then drying it. At that time, the Ag / AgCl paste is arranged so as to straddle the reference electrode 22b and the portion outside the probe 12 (the portion separated from the probe 12).
  • FIG. 17B is an enlarged view of the dotted line frame A31 portion of FIG. 17A (process C).
  • step D reference poles 22b, grooves A1 and A2, and Ag / AgCl paste formed on the substrate 21 are shown.
  • step D the head, tip, reagent layer 23, and film 25 of the probe 12 are not shown.
  • the first film 71 (a film different from the film 25) is attached on the sheet-shaped substrate 21.
  • the first film 71 has an opening in a portion where the reagent layer 23 is formed and a portion where the counter electrode 22c is exposed (for example, a portion in the region X3 shown in FIG. 14).
  • the opening of the portion of the first film 71 and the film 25 where the reagent layer 23 is formed may be referred to as the first opening.
  • the opening of the portion of the first film 71 and the film 25 where the counter electrode 22c is exposed may be referred to as a second opening.
  • the arrow A32 in FIG. 17B (step E) indicates the first opening of the first film 71.
  • the second opening of the first film 71 is not shown.
  • the contact angle with the liquid on the first film 71 is preferably higher than the contact angle with the liquid at the opening, and the larger the difference, the more preferable.
  • the diameter of the first opening of the first film 71 may be, for example, 2.5 mm. Further, in the first film 71, the second opening does not have to be formed.
  • Step F As shown in (Step F) of FIG. 17C, the reagent solution is applied to the first opening of the first film 71 attached to the sheet-shaped substrate 21, and the reagent layer 23 is formed.
  • Step G As shown in (Step G) of FIG. 17C, the reagent layer 23 and the electrode material portion (working electrode 22a) are trimmed (for trimming, refer to the first embodiment).
  • the probe 12 in the second embodiment does not have to be trimmed (step G).
  • Step H The first film 71 attached in step E is peeled off from the substrate 21. Then, as shown in (Step H) of FIG. 17C, the film 25 having the first opening and the second opening is attached to the sheet-shaped substrate 21. The first opening of the film 25 is located in the portion of the reagent layer 23, and the second opening is located in the portion of region X3 of the counter electrode 22c. The upper surface of the reference layer 24 is covered with the film 25. In (Step H) of FIG. 17C, the second opening of the film 25 is not shown.
  • the diameter of the first opening of the film 25 is larger than the diameter of the first opening of the first film 71, and may be, for example, 3.5 mm. That is, the first opening of the film 25 may have a size surrounding the reagent layer 23.
  • Step I As shown in (Step I) of FIG. 17D, ethanol 72 is applied to the first opening of the film 25.
  • ethanol 72 is applied to cover the first opening.
  • the diameter of the first opening is 3.5 mm
  • ethanol 72 of about 3 ul or more and 5 ul or less is applied.
  • the film 25 is formed by the contact angle formed by the liquid (in this case, ethanol 72) and the film 25 in contact with the film 25, and the liquid in the first opening (in this case, ethanol 72).
  • the material of the film 25 such that the contact angle of the former is larger. This is because the applied liquid (in this case, ethanol 72) is kept in the first opening so that the liquid does not leak from the first opening.
  • the larger the difference in contact angle between the two the more preferable.
  • the difference between the contact angles of the two is, for example, preferably 20 ° or more, more preferably 35 ° or more, and further preferably 50 ° or more.
  • step J As shown in (step J) of FIG. 17D, the protective film sheet 73 formed and cut in step A is arranged (placed) in the first opening of the film 25 as shown by arrow A33. Then, the ethanol 72 applied in step I is dried. As a result, the protective film sheet 73 is partially dissolved by ethanol 72 and dried, so that the first protective film 51 in close contact with the reagent layer 23 can be formed.
  • Step K As shown in (Step K) of FIG. 17E, the sheet-shaped substrate 21 is cut so as to have the shape of the probe 12.
  • Step L As shown in (Step L) of FIG. 17E, the cut probe 12 is dipped in a protective film solution (which may have a different composition) having the same composition as that of Step A and dried. The dipping and drying may be repeated, for example, at any number of times 1 or more and 3 or less. As a result, the second protective film 52 is formed on the probe 12.
  • a protective film solution which may have a different composition
  • the thickness of the second protective film 52 is preferably in the range of 5% or more and 60% or less of the thickness of the first protective film 51.
  • the thickness of the second protective film 52 is more preferably in the range of 10% or more and 50% or less, and further preferably in the range of 20% or more and 40% or less.
  • one dip is 1 ⁇ m or more and 4 ⁇ m or less, two dips are 2 ⁇ m or more and 8 ⁇ m or less, and three dips are 3 ⁇ m or more.
  • a second protective film 52 having a thickness of 12 ⁇ m or less can be formed.
  • Coating method 2a Structure of probe 12
  • the probe 12 manufactured by the coating method has basically the same structure as the probe 12 manufactured by the film pasting method. The differences in configuration will be described below.
  • FIG. 18 is a partial side view of the probe 12 on which the protective film is formed as viewed from the third surface side.
  • FIG. 19 is a top view of the tip portion of the probe 12 of FIG.
  • the shape of the first protective film 51 is different from the shape of the first protective film 51 (for example, see FIG. 15) formed by the film pasting method.
  • both ends of the first protective film 51 formed by the coating method rise in the direction along the insertion direction of the probe 12 into the living body.
  • the first protective film 51 has a convex shape at both ends in the direction in which the probe 12 is inserted into the living body.
  • the raised portion of the first protective film 51 may be referred to as an outer edge portion.
  • the width of the outer edge portion has a third predetermined distance as shown in FIG.
  • the region sandwiched between the outer edges of the first protective film 51 may be referred to as the inside.
  • the protective film solution is dropped onto the reagent layer 23 and dried to form the first protective film 51.
  • the protective film solution dries, a coffee ring is formed on the outer edge portion, so that the outer edge portion (raised portion) is formed on the first protective film 51.
  • the outer edge portion corresponds to a coffee ring, and the inside can be regarded as a portion other than the coffee ring.
  • the outer edge portion in the direction along the insertion direction of the probe 12 is separated (removed) from the probe 12.
  • the first protective film 51 is formed in a circular shape, for example, on the working electrode 22a that is not separated from the probe 12 (in other words, on the working electrode 22a that remains on the probe 12 after cutting).
  • a circular coffee ring (outer edge) is formed. That is, the outer edge portion of the first protective film 51 is included at least at both ends in the insertion direction of the probe 12 into the living body.
  • the first protective film 51 may be coated with the working electrode 22a including the reagent layer 23 as shown in FIG. 18, or may also be coated with the reference layer 24 as shown in FIG. 20.
  • FIG. 20 is a partial side view of the probe 12 on which the protective film is formed as viewed from the third surface side.
  • the same components as in FIG. 18 are designated by the same reference numerals.
  • the first protective film 51 may also cover the reference layer 24.
  • the film 25 may not be arranged on the upper surface of the reference layer 24.
  • the first protective film 51 may also cover the counter electrode 22c (counter electrode 22c of the region X3 portion) exposed from the film 25.
  • the reference electrode 22b or the counter electrode 22c is arranged on the same surface as the working electrode 22a.
  • 21A-21D are diagrams illustrating an example of a method for manufacturing the probe 12.
  • the electrode 22 is formed on the substrate 21 on the sheet.
  • an electrode material such as gold is sputtered onto a sheet-shaped substrate 21 such as polyethylene terephthalate (PET) to form an electrode 22.
  • PET polyethylene terephthalate
  • Step B As shown in (Step B) of FIG. 21A, the working electrode 22a, the reference electrode 22b, and the counter electrode 22c are formed. For example, laser processing is used to form the working pole 22a, the reference pole 22b, and the counterpole 22c. In FIG. 21A (step B), an example is shown in which the working electrode 22a, the reference electrode 22b, and the counter electrode 22c are formed on one surface.
  • the reference layer 24 is formed on the reference electrode 22b.
  • the reference layer 24 is formed by applying Ag / AgCl paste on the reference electrode 22b and then drying it. At that time, the Ag / AgCl paste straddles the reference electrode 22b and the portion outside the probe 12 (the portion separated from the probe 12) when the substrate 21 is cut in the cutting process of step K described later. Deploy.
  • Step D As shown in (Step D) of FIG. 21B, the first film 71 (a film different from the film 25) is attached on the sheet-shaped substrate 21.
  • the first film 71 has an opening in a portion where the reagent layer 23 is formed and a portion where the counter electrode 22c is exposed (for example, a portion in the region X3 shown in FIG. 18).
  • the opening of the portion of the first film 71 and the film 25 where the reagent layer 23 is formed may be referred to as the first opening.
  • the opening of the portion of the first film 71 and the film 25 where the counter electrode 22c is exposed may be referred to as a second opening.
  • the arrow A32 in FIG. 21B (step D) indicates the first opening.
  • the second opening is not shown.
  • the contact angle with the liquid on the first film 71 is preferably higher than the contact angle with the liquid at the opening, and the larger the difference, the more preferable.
  • the diameter of the first opening of the first film 71 may be, for example, 2.5 mm. Further, in the first film 71, the second opening does not have to be formed.
  • Step E As shown in (Step E) of FIG. 21B, the reagent solution is applied to the first opening of the first film 71 attached to the sheet-shaped substrate 21, and the reagent layer 23 is formed.
  • Step F As shown in (Step F) of FIG. 21C, the reagent layer 23 and the electrode material portion (working electrode 22a) are trimmed (for trimming, refer to the first embodiment).
  • the probe 12 in the second embodiment does not have to be trimmed (step F).
  • Step G The first film 71 attached in step D is peeled off from the substrate 21. Then, as shown in (Step G) of FIG. 21C, the film 25 having the first opening and the second opening is attached to the sheet-shaped substrate 21. The first opening of the film 25 is located in the portion of the reagent layer 23, and the second opening is located in the portion of region X3 of the counter electrode 22c. The upper surface of the reference layer 24 is covered with the film 25.
  • the diameter of the first opening of the film 25 is larger than the diameter of the first opening of the first film 71, and may be, for example, 3.2 mm. That is, the diameter of the first opening of the film 25 may have a size surrounding the reagent layer 23.
  • the protective film solution 74 is applied to the first opening of the film 25.
  • a protective film solution 74 that covers the first opening is applied.
  • the applied protective film solution 74 is dried to form the first protective film 51.
  • the film 25 includes a contact angle formed by the liquid (in this case, the protective film solution 74) and the film 25 in contact with the film 25, and the liquid in the first opening (in this case, the protective film solution 74).
  • the material of the film 25 such that the contact angle of the former is larger. This is because the applied liquid (in this case, the protective film solution 74) is kept in the first opening so that the liquid does not leak from the first opening.
  • the larger the difference in contact angle between the two the more preferable.
  • the difference between the contact angles of the two is, for example, preferably 20 ° or more, more preferably 35 ° or more, and further preferably 50 ° or more.
  • the protective membrane solution 74 is prepared by dissolving tBuMA4VP and poly (ethylene glucol) diglycidyl ether (hereinafter referred to as PEGDGE) as a cross-linking agent in ethanol so that the final concentrations are 8% and 0.62%, respectively. To create.
  • the drying temperature may be, for example, in the range of 10 ° C. or higher and 65 ° C. or lower. Drying may be performed, for example, for several minutes or more and several tens of minutes or less.
  • Step I As shown in (Step I) of FIG. 21D, the sheet-shaped substrate 21 is cut so as to have the shape of the probe 12.
  • Step J As shown in (Step J) of FIG. 21D, the cut probe 12 is dipped in a protective film solution (which may have a different composition) having the same composition as that of Step H and dried. The dipping and drying may be repeated, for example, at any number of times 1 or more and 3 or less. As a result, the second protective film 52 is formed on the probe 12.
  • a protective film solution which may have a different composition
  • the thickness of the second protective film 52 is preferably in the range of 5% or more and 60% or less of the thickness of the first protective film 51.
  • the thickness of the second protective film 52 is more preferably in the range of 10% or more and 50% or less, and further preferably in the range of 20% or more and 40% or less.
  • one dip is 1 ⁇ m or more and 4 ⁇ m or less, two dips are 2 ⁇ m or more and 8 ⁇ m or less, and three dips are 3 ⁇ m or more.
  • a second protective film 52 having a thickness of 12 ⁇ m or less can be formed.
  • FIG. 22 is a diagram illustrating a shape example of the first protective film 51 formed in step H.
  • FIG. 22 shows a top view of the first protective film 51 and a cross-sectional view taken along the line AA. Further, the dotted line X11 shown in FIG. 22 indicates a cut line to be cut in the step I.
  • the first protective film 51 has a circular coffee ring after the step H.
  • the probe 12 remains a portion of the circular coffee ring surrounded by the dotted frame X12. That is, the first protective film 51 has outer edges at both ends of the first protective film 51 in the direction of insertion of the probe 12 into the living body.
  • the probe 12 of the sensor 1 inserted into the living body and measuring the analyze includes the substrate 21, the electrode 22 formed on the substrate 21, and the reagent layer 23 formed on the electrode 22. It has a first protective film 51 formed on the reagent layer 23, and a second protective film 52 formed on the first protective film 51, which is thinner than the first protective film 51.
  • the senor 1 forms the first protective film 51 on the reagent layer 23, and forms the second protective film 52 thinner than the first protective film 51 on the first protective film 51, so that the reagent layer 23
  • the number of steps for forming the protective film is reduced, and variations in thickness and shape are suppressed. Therefore, the sensor 1 can be easily manufactured, and variations in performance are suppressed.
  • a sheet-shaped first protective film 51 having a predetermined thickness manufactured in advance is attached to a position including at least the reagent layer 23 portion of the probe 12.
  • a paste-like first protective film 51 having a predetermined thickness is applied to a position of the probe 12 including at least the reagent layer 23 portion.
  • the dip forming the second protective film 52 is one in which immersion and drying are repeated 1 or more and 5 or less, preferably 1 or more and 3 or less times, and the surface of the probe 12 of the first protective film 51 portion is covered. The number of times it can be covered may be sufficient.
  • the senor 1 can be easily manufactured by reducing the number of steps for forming the protective film of the reagent layer 23. Further, the sensor 1 can suppress variations in the thickness and shape of the protective film by forming a second protective film 52 thinner than the first protective film 51 on the first protective film 51 formed to be thick to some extent, and variations in performance. Can be suppressed.
  • a typical example is polyethylene phthalate as the substrate.
  • the material is not particularly limited as long as it is a resin material or a plastic material having flexibility, easy workability, and heat resistance.
  • Other examples include, for example, polyethylene, polypropylene, and polyethylene terephthalate-based general-purpose plastics.
  • polyimide is preferable.
  • the electrode material used for the working electrode and the counter electrode is not particularly limited as long as it is a metal or carbon material having conductivity and stability (hard to oxidize, salt resistance). Examples of such electrode materials include gold, platinum, palladium and carbon. When a metal material is used, the electrode material can be formed on the substrate by sputtering, vapor deposition, printing, plating, or spin coating.
  • electrodes When carbon is used, electrodes may be formed by screen printing using carbon paste.
  • the electrode materials on the first surface and the second surface may be the same or different electrode materials.
  • a plurality of counter electrodes may be provided.
  • both the first counter electrode (first counter electrode lead) and the second counter electrode (second counter electrode lead) may be provided on the first surface or the second surface, or the first counter electrode (first counter electrode lead) may be provided on the first surface. It may be provided on the surface and the second counter electrode (second counter electrode lead) may be provided on the second surface.
  • Reference layer Ag / AgCl may be used for the reference layer.
  • the insulating layer is formed of a film or resist ink. It is preferable to use a film that is basically the same material as the substrate and has an adhesive sheet (for example, acrylic type, rubber type, hot melt type) attached to the film. However, the adhesive sheet alone may be used as a film.
  • a thermal / thermoplastic resist film can be mentioned.
  • a general-purpose plastic film is used, and from the viewpoint of reagent application, a material having a contact angle with a liquid having a relationship of "contact angle of film surface> contact angle of film opening" is adopted.
  • the film opening referred to here refers to the surface of the working electrode before dropping and forming the reagent layer, that is, the first electrode material. Even if the material does not have such a contact angle, it is possible to have the relationship of the contact angle by treating the film surface with at least one of water-repellent treatment and hydrophilic treatment on the opening. ..
  • the film has a thickness selected from a range of approximately 1 ⁇ m or more and 250 ⁇ m or less, preferably 3 ⁇ m or more and 50 ⁇ m or less, and more preferably 5 ⁇ m or more and 30 ⁇ m or less.
  • the insulating layer it is preferable to use a film as described in the first embodiment and the second embodiment rather than forming the insulating layer with resist ink.
  • the reagent layer contains at least an oxidoreductase that undergoes a redox reaction with analite.
  • the reagent layer may or may not include an electron mediator (a system for detecting generated hydrogen peroxide). May be good.
  • an electron mediator is included in the reagent layer.
  • bioprotective film The bioprotective membrane prevents or suppresses the leakage of substances (mainly oxidoreductases) contained in the reagent layer to the outside of the protective membrane, and the reagent layer contains analysts existing outside the protective membrane. It has a permeable hole in the protective film. Therefore, the bioprotective film is not particularly limited as long as it is a polymer having such a function.
  • the bioprotective film needs to be arranged so as to cover at least the reagent layer. Furthermore, since the sensor probe is used by inserting it into the living body, the bioprotective film covering the surface thereof generally has biocompatibility in which proteins and cells do not adsorb or are difficult to adsorb. Preferably employs a polymer having such properties.
  • the polymer used for the bioprotective film may be either a polymer composed of a single monomer or a copolymer composed of two or more kinds of monomers. Further, as the copolymer, a copolymer composed of any of random copolymerization, alternating copolymerization and block copolymerization may be adopted.
  • the polymer preferably has a degree of polymerization of 100 or more and a molecular weight in the range of 10,000 or more and 1,000,000 or less, more preferably 30,000 or more and 500,000 or less, and 50. More preferably, it is in the range of 000 or more and 200,000 or less.
  • the ratio of the two structural skeletons is the first.
  • the ratio of the second structural skeleton is preferably in the range of 25 or more and 400 or less, more preferably in the range of 50 or more and 200 or less, and more preferably in the range of 75 or more and 150 or less. ..
  • the ratio of the three structural skeletons is the first.
  • the ratio of the second structural skeleton and the third structural skeleton is preferably in the range of 1 or more and 400 or less, more preferably in the range of 3 or more and 100 or less, and 5 or more and 50 or less. The one in the range of is more preferable.
  • the polymer (including not only the copolymer but also the polymer composed of a single monomer) is preferably a polymer containing a heterocyclic compound as the first structural skeleton, and more preferably a heteroatom heterocyclic compound. It is preferably present, and more preferably a nitrogen-containing heterocyclic compound.
  • Such polymers include polyurethane, silicone-based polymers, polytetrafluoroethylene, polyethylene-co-tetrafluoroethylene, polypropylene, and poly, as long as they are other than polymers having a nitrogen-containing heterocyclic compound as the first structural skeleton.
  • examples thereof include vinyl chloride, polyvinylidene fluoride, polybutylene terephthalate, polymethylmethacrylate, polyether ether ketone, polyurethane, cellulose-based polymer, and polysulfone.
  • a polymer containing a nitrogen-containing heterocyclic compound as the first structural skeleton will be described.
  • the polymer composed of a single monomer include polyvinyl pyridines having vinyl pyridines as the first structural skeleton.
  • examples thereof include polyvinyl imidazoles having vinyl imidazoles as the first structural skeleton.
  • Specific compounds of this example include, for example, poly (4-vinylpyridine), poly (3-vinylpyridine), poly (2-vinylpyridine) as polyvinylpyridines, and poly (1) as vinylimidazoles.
  • -Vinyl imidazole poly (2-vinyl imidazole), poly (4-vinyl imidazole) and the like.
  • those having the first and second structural skeletons include, for example, those having styrenes and methacrylates as the second structural skeleton.
  • Specific compounds of this example include, for example, poly (tert-butyl methacrylate-b-poly (4-vinylpyridine)).
  • those composed of the first, second and third structural skeletons include styrenes as the third structural skeleton (when the second structural skeleton is methacrylate). And methacrylates (when the second structural skeleton is styrene).
  • Specific compounds of this example include, for example, poly (styrene-co-4-vinylpyridine-co-oligo [(propylene glycol methyl ether methacrylate) random] and the like.
  • a cross-linking agent to covalently bond the polymers.
  • a cross-linking agent By using a cross-linking agent, a mesh as a bioprotective film is formed, the swelling of the bioprotective film is prevented due to the use of a sensor for a long period of time, the shape of the bioprotective film is maintained, and the permeability of glucose is kept constant. This is because it is considered to be useful for keeping.
  • the cross-linking agent it is also possible for the cross-linking agent to have a certain function.
  • PEGDGE more specifically, PEGDGE1000
  • this PEGDGE has a role of imparting hydrophilicity to the bioprotective film.
  • the cross-linking agent to be used and the amount to be added thereof can be appropriately selected depending on the polymer to be used, but it is necessary to use a cross-linking agent having a molecular structure having at least two glycidyl groups, as a specific example.
  • examples include poly (ethylene glycol) diglycidyl ester and poly (propylene glycol) diglycidyl ester.
  • redox enzymes include glucose oxidase and glucose dehydrogenase.
  • glucose dehydrogenase FAD-bound glucose dehydrogenase is desirable from the viewpoint of low reactivity with maltose, and for example, FAD-bound glucose dehydrogenase of the genus Aspergillus (Orize or Tereus) or Mucor is preferable.
  • Electrode examples include osmium complex, ruthenium complex, quinone compound, phenazine compound, ferrocene compound and the like, and derivatives thereof.
  • an oxidase-based oxidoreductase is used and no electronic mediator is used, hydrogen peroxide produced by the reaction with glucose is detected.
  • the electronic mediator may be configured to be bonded to the polymer via a linker. This configuration is preferable for preventing / suppressing the outflow of the electronic mediator to the outside of the protective film (so-called in-vivo) when configuring the embedded electrochemical sensor (having a protective film).
  • the width of the probe is preferably in the range of about 70 ⁇ m or more and 1700 ⁇ m or less in consideration of embedding in a living body. It is preferably 70 ⁇ m or more and 600 ⁇ m or less, and more preferably 70 ⁇ m or more and 400 ⁇ m or less.
  • each component in the embodiment may be arbitrarily combined as long as the purpose of the present disclosure is not deviated.
  • the probe 12 described in the second embodiment may have a trimming portion formed in the same manner as the probe 12 described in the first embodiment.
  • a part of the film 25 may be overlapped on the reagent layer 23 at both ends in the insertion direction of the reagent layer 23. .. Further, the film 25 on the insertion direction side does not have to be formed.
  • the present disclosure is useful for biosensors, such as CGM sensors.

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PCT/JP2021/007534 2020-02-28 2021-02-26 センサーおよびその製造方法 WO2021172564A1 (ja)

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JP2012519038A (ja) * 2009-02-26 2012-08-23 アボット ダイアベティス ケア インコーポレイテッド 改良された検体センサおよびその製造および使用方法
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US20230105478A1 (en) 2023-04-06
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JP7316437B2 (ja) 2023-07-27
JPWO2021172564A1 (enrdf_load_stackoverflow) 2021-09-02

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